首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Synthesis, structure and inclusion properties of cone-tris{[(5'-methyl-2,2'-bipyridyl)-5-yl]oxycarbonylmethoxy}hexahomotrioxacalix[3]arene
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Synthesis, structure and inclusion properties of cone-tris{[(5'-methyl-2,2'-bipyridyl)-5-yl]oxycarbonylmethoxy}hexahomotrioxacalix[3]arene

机译:锥-三{[((5'-甲基-2,2'-联吡啶基)-5-基]氧羰基甲氧基}六高三氧杂lix [3]芳烃的合成,结构和包合性质

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摘要

Hexahomotrioxacalix[3]arene having [(5'-methyl-2,2'-bipyridyl)-5-yl]oxycarbonylmethoxy group with cone conformation was prepared, which shows strong Ag~+ affinity and acts as a ditopic receptor for Ag~+ and nBuNH3~+. A conformational change of 2,2'-bipyridyl moiety from the original outward orientation of the ring nitrogen to the inside orientation toward the thiacalixarene cavity was observed in the process of Ag~+ complexation.
机译:制备具有[(5'-甲基-2,2'-联吡啶基)-5-基]氧羰基甲氧基的具有六聚体构象的六亚甲基三氧杂lix [3]亚芳基,其显示出强的Ag〜+亲和力并充当Ag〜+的二位受体和nBuNH3〜+。在Ag〜+络合过程中观察到了2,2'-联吡啶基部分的构象变化,即从环氮的原始向外取向到向噻菌素腔的内部取向。

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